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CAS号：246539-15-1|Dibotermin alfa
作者：德尔塔 日期：2022-12-23
中文别名：Dibotermin alfa英文别名：Dibotermin alfaCAS号：246539-15-1SMILES：Inchi：InchiKey：分子式 Formula：分子量 Molecular Weight：闪点 FP：NA熔点 Melting point：NA沸点 Boiling point：NAPolarizability极化度：密度 Density：NA蒸汽压 Vapor Pressure：溶解度Solubility：性状：NA储藏条件 Storage conditions：Dibotermin alfa使用注意事项：1.实验前需戴好防护眼镜，穿戴防护服和口罩，佩戴手套，避免与皮肤接触。2.实验过程中如遇到有毒或者刺激性物质及有害物质产生，必要时实验操作需要手套箱内完成以免对实验人员造成伤害。3.取样品的移液枪头需及时更换，必要时为避免交叉污染尽可能选择滤芯吸头。4.称量药品时选用称量纸，并无风处取药和称量以免扬撒，试剂的容器使用前务必确保干净，并消毒。5.取药品时尽量采用多个药勺分别使用，使用后清洗干净。6.实验后产生的废弃物需分类存储，并交于专业生物废气物处理公司处理，以免造成环境污染。大规格定制：定制产品请将信息发送至sales@bio-fount.com。Experimental considerations: 1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment. 2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.产品说明Organic Acids Introduction Application1In the same pathway shared by endogenous BMPs, recombinant human BMP-2 (rhBMP-2) binds and initiates intracellular signal cascade through an oligomeric transmembrane receptor complex formed by type I and II serine/threonine kinase receptor proteins4. These BMP receptors are expressed on the surface of mesenchymal cells and upon binding of BMP-2 to the BMP re
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CAS号：263870-19-5|APC-6336
作者：德尔塔 日期：2022-12-23
中文别名：APC-6336英文别名：APC-6336; APC 6336; APC6336; UNII-4124YUO44Z; CRA-6336; 4124YUO44Z;CAS号：263870-19-5SMILES：Cn1c2cc(ccc2nc1Cc3[nH]c4ccc(cc4n3)C(=O)N)C(=O)N[C@@H](CP(=O)(O)O)C(=O)OInchi：InChI=1S/C21H21N6O7P/c1-27-16-7-11(20(29)26-15(21(30)31)9-35(32,33)34)3-5-13(16)25-18(27)8-17-23-12-4-2-10(19(22)28)6-14(12)24-17/h2-7,15H,8-9H2,1H3,(H2,22,28)(H,23,24)(H,26,29)(H,30,31)(H2,32,33,34)/t15-/m0/s1InchiKey：PEXFKSJDXSBOLP-HNNXBMFYSA-N分子式 Formula：C21H21N6O7P分子量 Molecular Weight：500.4闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明APC-6336(CAS:263870-19-5):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionAPC-6336 is a bio-active chemical. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注。订购说明：1、绝大部分产品备有现货，一般情况下都能订货当日发货。2、部分非常用产品，需提前1－2日预订，海外期货则需要提前3-6周预订。3、部分产品价格会因货期、批次等因素发生变化，若有变动以订货当日新价格为准。4、每日订单截止时间为16点整，部分城市可到17点整，因超过截止时间造成当日不能发货的将于次日安排发货。运输说明：极低温产品：极低温产品运输过程中加装干冰运输。用干冰把产品包裹起来，再用泡沫盒密封，胶带层层粘住泡沫盒，放入德尔塔生物的箱子，然后交付给合作快递，安全快速高效放心的送至客户的手中，保证产品的性质稳定如一，为您的实验保驾护航
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CAS号：62003-89-8|Aplysistatin
作者：德尔塔 日期：2022-12-23
中文别名：Aplysistatin英文别名：AplysistatinCAS号：62003-89-8SMILES：C12=CC[C@H]3C([C@H](CC[C@]3(C)O[C@H]2COC1=O)Br)(C)CInchi：InChI=1S/C15H21BrO3/c1-14(2)11-5-4-9-10(8-18-13(9)17)19-15(11,3)7-6-12(14)16/h4,10-12H,5-8H2,1-3H3/t10-,11-,12-,15-/m0/s1InchiKey：BEMNKPXNGWTBLQ-ASHKBJFXSA-N分子式 Formula：C15H21BrO3分子量 Molecular Weight：329.23闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明Aplysistatin(CAS:62003-89-8):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionAplysistatin is a bromosesquiterpene derived from sea mollusks. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Couladouros EA, Vidali VP. Novel stereocontrolled approach to syn- and anti-oxepene-cyclogeranyl trans-fused polycyclic systems: asymmetric total synthesis of (-)-Aplysistatin, (+)-Palisadin A, (+)-Palisadin B, (+)-12-hydroxy-palisadin B, and the AB ring system of adociasulfate-2 and toxicol A. Chemistry. 2004 Aug 6;10(15):3822-35. PubMed PMID: 15281167.[2]Koshimura M, Utsukihara T, Kawamoto M, Saito M, Horiuchi CA, Kuniyoshi M. Biotransformation of bromosesquiterpenes by marine fungi. Phytochemistry. 2009 Dec;70(17-18):2023-6. doi: 10.1016/j.phytochem.2009.08.021. Epub 2009 Sep 21. PubMed PMID: 19772936.[3] Pettit GR, Herald CL, Allen MS, von Dreele RB,
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CAS号：60925-00-0|Apoptosis inducer 5d
作者：德尔塔 日期：2022-12-23
中文别名：Apoptosis inducer 5d英文别名：Apoptosis inducer 5dCAS号：60925-00-0SMILES：BrC1=CC=C(N2N=C(C3=CC=CN=C3)C=C2C4=CC=CC=C4)C=C1Inchi：InChI=1S/C20H14BrN3/c21-17-8-10-18(11-9-17)24-20(15-5-2-1-3-6-15)13-19(23-24)16-7-4-12-22-14-16/h1-14HInchiKey：TZHWETVMXQTIER-UHFFFAOYSA-N分子式 Formula：C20H14BrN3分子量 Molecular Weight：376.257闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明Apoptosis inducer 5d(CAS:60925-00-0):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionApoptosis inducer 5d is a novel inducer of cell death by activating apoptosis in cancer cells. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Fernández-Laso V, Sastre C, Valdivielso JM, Betriu A, Fernández E, Egido J, Martín-Ventura JL, Blanco-Colio LM. Soluble TWEAK and Major Adverse Cardiovascular Events in Patients with CKD. Clin J Am Soc Nephrol. 2016 Mar 7;11(3):413-22. doi: 10.2215/CJN.07900715. Epub 2016 Jan 4. PubMed PMID: 26728587; PubMed Central PMCID: PMC4791813.[2]Kemnitzer W, Sirisoma N, May C, Tseng B, Drewe J, Cai SX. Discovery of 4-anilino-N-methylthieno[3,2-d]pyrimidines and 4-anilino-N-methylthieno[2,3-d]pyrimidines as potent apoptosis inducers. Bioorg Med Chem Lett. 2009 Jul 1;19(13):3536-40. doi: 10.1016/j.bmcl.2009.04.145. Epub 2009 May 5.
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CAS号：669770-29-0|AQW051
作者：德尔塔 日期：2022-12-23
中文别名：AQW051英文别名：AQW051; AQW-051; AQ W051CAS号：669770-29-0SMILES：CC1=CC=C(C2=CC=C(O[C@H]3CN4CCC3CC4)C=N2)C=C1Inchi：InChI=1S/C19H22N2O/c1-14-2-4-15(5-3-14)18-7-6-17(12-20-18)22-19-13-21-10-8-16(19)9-11-21/h2-7,12,16,19H,8-11,13H2,1H3/t19-/m0/s1InchiKey：NPDLTEZXGWRMLQ-IBGZPJMESA-N分子式 Formula：C19H22N2O分子量 Molecular Weight：294.398闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明AQW051(CAS:669770-29-0):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionAQW051 is a novel, potent and selective α7 nicotinic ACh receptor partial agonist. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Barch DM, Marder SR, Harms MP, Jarskog LF, Buchanan RW, Cronenwett W, Chen LS, Weiss M, Maguire RP, Pezous N, Feuerbach D, Lopez-Lopez C, Johns DR, Behrje RB, Gomez-Mancilla B. Task-related fMRI responses to a nicotinic acetylcholine receptor partial agonist in schizophrenia: A randomized trial. Prog Neuropsychopharmacol Biol Psychiatry. 2016 Nov 3;71:66-75. doi: 10.1016/j.pnpbp.2016.06.013. PubMed PMID: 27371157.[2]Welsh KJ, Bai Y; Education Committee of the Academy of Clinical Laboratory Physicians and Scientists.. Pathology Consultation on Patients With a Large Rh Immune Globulin Dose Requirement. Am J Clin Pathol. 2016 Jun;145(6)
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CAS号：62715-01-9|AR 03 Cl
作者：德尔塔 日期：2022-12-23
中文别名：AR 03 Cl英文别名：AR 03 ClCAS号：62715-01-9SMILES：CC1(c2ccccc2C(=O)N(C1=O)CCCNCCCN3C(=O)c4ccccc4C(C3=O)(C)C)CInchi：1S/C28H33N3O4/c1-27(2)21-13-7-5-11-19(21)23(32)30(25(27)34)17-9-15-29-16-10-18-31-24(33)20-12-6-8-14-22(20)28(3,4)26(31)35/h5-8,11-14,29H,9-10,15-18H2,1-4H3InchiKey：BVBLBGFQYTUFKY-UHFFFAOYSA-N分子式 Formula：C28H33N3O4分子量 Molecular Weight：475.59闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明AR 03 Cl(CAS:62715-01-9):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionAR 03 Cl is an anti-arhythmic which causes a significant prolongation in conduction. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Gülker H, Spyra W, Thale J, Krimphove F, Hübner A, Bender F. Assessment of the electrophysiologic, antiarrhythmic and haemodynamic profile of a new isoquinolinedione derivative. Arzneimittelforschung. 1987 Aug;37(8):917-9. PubMed PMID: 3675686.订购说明：1、绝大部分产品备有现货，一般情况下都能订货当日发货。2、部分非常用产品，需提前1－2日预订，海外期货则需要提前3-6周预订。3、部分产品价格会因货期、批次等因素发生变化，若有变动以订货当日新价格为准。4、每日订单截止时间为16点整，部分城市可到17点整，因超过截止时间造成当日不能发货的将于次日安排发货。运输说明：极低温产品：极低温产品运输过程中加装干冰运输。用干冰
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CAS号：100557-06-0|AR 12456
作者：德尔塔 日期：2022-12-23
中文别名：AR 12456英文别名：AR 12456; AR-12456; AR12456CAS号：100557-06-0SMILES：c1c(nc2ncnn2c1N(CCCCCC)CCO)N(CC)CCInchi：InChI=1S/C17H30N6O/c1-4-7-8-9-10-22(11-12-24)16-13-15(21(5-2)6-3)20-17-18-14-19-23(16)17/h13-14,24H,4-12H2,1-3H3InchiKey：NWCVGIMEZSWINX-UHFFFAOYSA-N分子式 Formula：C17H30N6O分子量 Molecular Weight：334.46闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明AR 12456(CAS:100557-06-0):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionAR-12456 is a trapidil derivative. AR 12456 protects against serum hyperlipidemia in guinea pigs. AR 12456 has a strong antilipidemic action in guinea pigs fed a cholesterol-rich diet. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Corsini A, Grignaffini P, Beitz J, Mest H, Bellosta S, Fumagalli R, Paoletti R. Effect of trapidil derivative AR 12456 on intracellular cholesterol homeostasis in human hepatoma cell line Hep G2. Cytotechnology. 1993 Jan;11(Suppl 1):S15-7. doi: 10.1007/BF00746043. PubMed PMID: 22358683.[2]Corsini A, Grignaffini P, Beitz J, Mest HJ, Bellosta S, Fumagalli R, Paoletti R. Effect of trapidil derivative AR 12456 on intracellular cholesterol homeostasis in human hepatoma cell line Hep G2. Cytotechnology. 1993;11 Suppl 1:S15-7. PubMed PMID: 7763747.[3] Beitz
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CAS号：100557-07-1|AR 12465
作者：德尔塔 日期：2022-12-23
中文别名：AR 12465英文别名：AR 12465, AR-12465CAS号：100557-07-1SMILES：CCCCCCN(CCO)c1cc(nc2ncnn12)N3CCCCC3Inchi：1S/C18H30N6O/c1-2-3-4-6-11-23(12-13-25)17-14-16(22-9-7-5-8-10-22)21-18-19-15-20-24(17)18/h14-15,25H,2-13H2,1H3InchiKey：CAUSJFJJYRCTPJ-UHFFFAOYSA-N分子式 Formula：C18H30N6O分子量 Molecular Weight：346.48闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明AR 12465(CAS:100557-07-1):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionAR 12465 is a trapidil derivative which may affect LDL receptor mediated uptake and degradation of 125 I-LDL by human skin fibroblasts (HSF) and human hepatic cells (HEP G2). Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Beitz J, Corsini A, Granata A, Fumagalli R, Mest HJ, Paoletti R. Effect of derivatives of trapidil on the expression of LDL receptors. Biomed Biochim Acta. 1988;47(10-11):S153-6. PubMed PMID: 2854727.订购说明：1、绝大部分产品备有现货，一般情况下都能订货当日发货。2、部分非常用产品，需提前1－2日预订，海外期货则需要提前3-6周预订。3、部分产品价格会因货期、批次等因素发生变化，若有变动以订货当日新价格为准。4、每日订单截止时间为16点整，部分城市可到17点整，因超过截止时间造成当日不能发货的将于次日安排发货。运输说明：极低温产品：极低温产品运输过程中加装干冰运输。用干冰把产品包裹起
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CAS号：83162-82-7|Arcapillin
作者：德尔塔 日期：2022-12-23
中文别名：Arcapillin英文别名：ArcapillinCAS号：83162-82-7SMILES：O=C1C=C(C2=CC(OC)=C(O)C=C2O)OC3=C1C(O)=C(OC)C(OC)=C3Inchi：InChI=1S/C18H16O8/c1-23-13-4-8(9(19)5-10(13)20)12-6-11(21)16-14(26-12)7-15(24-2)18(25-3)17(16)22/h4-7,19-20,22H,1-3H3InchiKey：IZWKTABKAJGBFW-UHFFFAOYSA-N分子式 Formula：C18H16O8分子量 Molecular Weight：360.318闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明Arcapillin(CAS:83162-82-7):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionArcapillin is an anticancer agent, inducing apoptosis mediated at least in part by the ERS pathway and inhibiting hepatoma tumor growth. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Nurul Islam M, Jung HA, Sohn HS, Kim HM, Choi JS. Potent α-glucosidase and protein tyrosine phosphatase 1B inhibitors from Artemisia capillaris. Arch Pharm Res. 2013 May;36(5):542-52. doi: 10.1007/s12272-013-0069-7. Epub 2013 Feb 24. PubMed PMID: 23435948.[2]Jung HA, Park JJ, Islam MN, Jin SE, Min BS, Lee JH, Sohn HS, Choi JS. Inhibitory activity of coumarins from Artemisia capillaris against advanced glycation endproduct formation. Arch Pharm Res. 2012 Jun;35(6):1021-35. doi: 10.1007/s12272-012-0610-0. Epub 2012 Jun 30. PubMed PMID: 22870812.[3] Lin S, Zhang QW, Zhang NN, Zhang YX. [Determi
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CAS号：60173-73-1|Arfalasin
作者：德尔塔 日期：2022-12-23
中文别名：Arfalasin英文别名：Arfalasin; Arfalasinum; Arfalasine;CAS号：60173-73-1SMILES：CC([C@@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N1CCC[C@H]1C(N[C@@H](c2ccccc2)C(O)=O)=O)=O)Cc3nc[nH]c3)=O)C(C)C)=O)Cc4ccc(O)cc4)=O)NC([C@@H](NC(CCC(N)=O)=O)CCCNC(N)=N)=O)CInchi：1S/C48H67N13O11/c1-26(2)38(58-41(65)32(12-8-20-53-48(50)51)55-37(64)19-18-36(49)63)44(68)56-33(22-28-14-16-31(62)17-15-28)42(66)59-39(27(3)4)45(69)57-34(23-30-24-52-25-54-30)46(70)61-21-9-13-35(61)43(67)60-40(47(71)72)29-10-6-5-7-11-29/h5-7,10-11,14-17,24-27,32-35,38-40,62H,8-9,12-13,18-23H2,1-4H3,(H2,49,63)(H,52,54)(H,55,64)(H,56,68)(H,57,69)(H,58,65)(H,59,66)(H,60,67)(H,71,72)(H4,50,51,53)/t32-,33-,34-,35-,38-,39-,40-/m0/s1InchiKey：IBGNPQRJAXAGJH-MBNHCIONSA-N分子式 Formula：C48H67N13O11分子量 Molecular Weight：1002.14闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明Arfalasin(CAS:60173-73-1):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionArfalasin is a bioactive chemical. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Imbs JL, Schmidt M, Giesen EM, Schwartz J. Is the renin-angiotensin system involved in urinary concentration mechanisms? J Physiol (Paris). 1984;79(6):481-4. PubMed PMID: 6399315.订购说明：1、绝大部分产品备有现货，一般情况下都能订货当日发货。2、部分非
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CAS号：108890-87-5|Arizonin A1
作者：德尔塔 日期：2022-12-23
中文别名：Arizonin A1英文别名：Arizonin A1CAS号：108890-87-5SMILES：O=C(O1)C[C@]2([H])[C@@]1([H])C(C3=O)=C(C(C4=C3C=CC(O)=C4OC)=O)[C@@H](C)O2Inchi：InChI=1S/C17H14O7/c1-6-11-13(17-9(23-6)5-10(19)24-17)14(20)7-3-4-8(18)16(22-2)12(7)15(11)21/h3-4,6,9,17-18H,5H2,1-2H3/t6-,9-,17+/m1/s1InchiKey：VQAHDQIOJTXEAY-WEWYWXMASA-N分子式 Formula：C17H14O7分子量 Molecular Weight：330.29闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明Arizonin A1(CAS:108890-87-5):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionArizonin A1 is a biochemical. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注。订购说明：1、绝大部分产品备有现货，一般情况下都能订货当日发货。2、部分非常用产品，需提前1－2日预订，海外期货则需要提前3-6周预订。3、部分产品价格会因货期、批次等因素发生变化，若有变动以订货当日新价格为准。4、每日订单截止时间为16点整，部分城市可到17点整，因超过截止时间造成当日不能发货的将于次日安排发货。运输说明：极低温产品：极低温产品运输过程中加装干冰运输。用干冰把产品包裹起来，再用泡沫盒密封，胶带层层粘住泡沫盒，放入德尔塔生物的箱子，然后交付给合作快递，安全快速高效放心的送至客户的手中，保证产品的性质稳定如一，为您的实验保驾护航。低温产品：低温产品运输过程中加装冰袋运输。事先用冰袋把产品包裹起来，再使用泡沫盒密封，用胶带严实密封泡沫盒，再放入德尔塔生物的箱子
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CAS号：153994-97-9|CGP 56999A
作者：德尔塔 日期：2022-12-23
中文别名：CGP 56999A英文别名：CGP 56999A; CGP56999A; CGP-56999A .CAS号：153994-97-9SMILES：O=C(O)C1=CC=CC([C@H](NC[C@H](O)CP(OC2CCCCC2)(C)=O)C)=C1Inchi：InChI=1S/C19H30NO5P/c1-14(15-7-6-8-16(11-15)19(22)23)20-12-17(21)13-26(2,24)25-18-9-4-3-5-10-18/h6-8,11,14,17-18,20-21H,3-5,9-10,12-13H2,1-2H3,(H,22,23)/t14-,17+,26?/m1/s1InchiKey：NLWRVVKVUYDPTH-ZIYGTXEKSA-N分子式 Formula：C19H30NO5P分子量 Molecular Weight：383.42闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明CGP 56999A(CAS:153994-97-9):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionCGP 56999A is a GABA(B) receptor antagonist, which enhances expression of brain-derived neurotrophic factor and attenuates dopamine depletion in the rat corpus striatum. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Enna SJ, Reisman SA, Stanford JA. CGP 56999A, a GABA(B) receptor antagonist, enhances expression of brain-derived neurotrophic factor and attenuates dopamine depletion in the rat corpus striatum following a 6-hydroxydopamine lesion of the nigrostriatal pathway. Neurosci Lett. 2006 Oct 2;406(1-2):102-6. PubMed PMID: 16890350.[2]Tsai ML, Crutchley M, Boyce R, Ma J, Boon F, Cain DP, Leung LS. Long-lasting auditory gating deficit accompanied by GABA(B) receptor dysfunction in th
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CAS号：150608-41-6|Cgp 57813
作者：德尔塔 日期：2022-12-23
中文别名：Cgp 57813英文别名：Cgp 57813; Cgp-57813; Cgp57813.CAS号：150608-41-6SMILES：C(N[C@H](C(N1CCOCC1)=O)Cc1ccccc1)([C@@H](NC([C@@H](C[C@@H]([C@@H](NC(OC(C)(C)C)=O)Cc1ccccc1)O)Cc1ccc(cc1)OC)=O)C(C)C)=OInchi：InChI=1S/C43H58N4O8/c1-29(2)38(40(50)44-36(27-31-15-11-8-12-16-31)41(51)47-21-23-54-24-22-47)46-39(49)33(25-32-17-19-34(53-6)20-18-32)28-37(48)35(26-30-13-9-7-10-14-30)45-42(52)55-43(3,4)5/h7-20,29,33,35-38,48H,21-28H2,1-6H3,(H,44,50)(H,45,52)(H,46,49)/t33-,35+,36+,37+,38+/m1/s1InchiKey：DZUIFTBFVIXAMZ-YHKVADFHSA-N分子式 Formula：C43H58N4O8分子量 Molecular Weight：758.94闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明Cgp 57813(CAS:150608-41-6):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionCGP 57813 is a lipophilic compound that acts as a inhibitor of human immunodeficiency virus type 1 (HIV-1) protease. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Leroux JC, Cozens RM, Roesel JL, Galli B, Doelker E, Gurny R. pH-sensitive nanoparticles: an effective means to improve the oral delivery of HIV-1 protease inhibitors in dogs. Pharm Res. 1996 Mar;13(3):485-7. PubMed PMID: 8692747.[2]Leroux JC, Cozens R, Roesel JL, Galli B, Kubel F, Doelker E, Gurny R. Pharmacokinetics of a novel HIV-1 protease inhibitor incorporate
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CAS号：187608-26-0|CGP 62349
作者：德尔塔 日期：2022-12-23
中文别名：CGP 62349英文别名：CGP 62349; CGP-62349; CGP62349.CAS号：187608-26-0SMILES：O=C(O)C1=CC=CC([C@H](N(C[C@H](O)CP(CC2=CC=C(OC)C=C2)(O)=O)C)C)=C1Inchi：InChI=1S/C21H28NO6P/c1-15(17-5-4-6-18(11-17)21(24)25)22(2)12-19(23)14-29(26,27)13-16-7-9-20(28-3)10-8-16/h4-11,15,19,23H,12-14H2,1-3H3,(H,24,25)(H,26,27)/t15-,19+/m1/s1InchiKey：AKUSEWDIEMJQBM-BEFAXECRSA-N分子式 Formula：C21H28NO6P分子量 Molecular Weight：421.43闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明CGP 62349(CAS:187608-26-0):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionCGP 62349 is a GABAB receptor antagonist. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：[1]Keir MJ, Barakat MJ, Dev KK, Bittiger H, Bettler B, Henley JM. Characterisation and partial purification of the GABA(B) receptor from the rat cerebellum using the novel antagonist [3H]CGP 62349. Brain Res Mol Brain Res. 1999 Aug 25;71(2):279-89. PubMed PMID: 10521582.[2]Ambardekar AV, Ilinsky IA, Forestl W, Bowery NG, Kultas-Ilinsky K. Distribution and properties of GABA(B) antagonist [3H]CGP 62349 binding in the rhesus monkey thalamus and basal ganglia and the influence of lesions in the reticular thalamic nucleus. Neuroscience. 1999;93(4):1339-47. PubMed PMID: 10501458.订购说明：1、绝大部分产品备有
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CAS号：200402-50-2|CGP 64213
作者：德尔塔 日期：2022-12-23
中文别名：CGP 64213英文别名：CGP 64213; CGP-64213; CGP64213.CAS号：200402-50-2SMILES：O=C(O)C1=CC=CC([C@H](NC[C@H](O)CP(CCCCCNC(CCC2=CC=C(O)C(I)=C2)=O)(O)=O)C)=C1Inchi：InChI=1S/C26H36IN2O7P/c1-18(20-6-5-7-21(15-20)26(33)34)29-16-22(30)17-37(35,36)13-4-2-3-12-28-25(32)11-9-19-8-10-24(31)23(27)14-19/h5-8,10,14-15,18,22,29-31H,2-4,9,11-13,16-17H2,1H3,(H,28,32)(H,33,34)(H,35,36)/t18-,22+/m1/s1InchiKey：RLYLJDJFHZHCTR-GCJKJVERSA-N分子式 Formula：C26H36IN2O7P分子量 Molecular Weight：646.46闪点 FP：熔点 Melting point：沸点 Boiling point：Polarizability极化度：密度 Density：蒸汽压 Vapor Pressure：溶解度Solubility：性状：Solid powder储藏条件 Storage conditions：Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).产品说明CGP 64213(CAS:200402-50-2):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。 IntroductionCGP 64213 is a GABAb receptor agonist. Application1Application2 Application3危险性：Warning危险性警示：安全声明：安全防护：备注：2: Duthey B, Caudron S, Perroy J, Bettler B, Fagni L, Pin JP, Prézeau L. A single subunit (GB2) is required for G-protein activation by the heterodimeric GABA(B) receptor. J Biol Chem. 2002 Feb 1;277(5):3236-4[1]PubMed PMID: 11711539; PubMed Central PMCID: PMC2566549.3: Calon F, Lavertu N, Lemieux AM, Morissette M, Goulet M, Grondin R, Blanchet PJ, Bédard PJ, Di Paolo T. Effect of MPTP-induced denervation on basal ganglia GABA(B) receptors: correlation with dopamine concentrations and dopamine transporter. Synapse. 2001 Jun 1;40(3):225-34
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